Catalog No.
Product Name
Application
Product Information
Citations
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Adenosine Analog
5-Methyl-4’-thiouridine is an adenosine analog that primarily targets adenosine receptors. This compound exhibits significant vasodilatory effects, promoting smooth muscle relaxation, and has shown potential in inhibiting cancer progression. Its applications in research encompass studies on cardiovascular function and cancer therapeutics. -
Purine Nucleoside Analog
2'-Deoxy-N2,N2-diethyl guanosine is a purine nucleoside analog that exhibits significant antitumor activity, particularly against indolent lymphoid malignancies. Its primary mechanism involves the inhibition of DNA synthesis and the induction of apoptosis, making it a valuable tool in cancer research. This compound is essential for studies focused on the therapeutic potential of nucleoside analogs in oncology. -
Guanosine 5'-Phosphate
7-Methyl-guanosine-5'-triphosphate disodium is a modified guanosine 5'-phosphate that plays a critical role in cellular signaling and protein synthesis. As a potent cap-dependent translation inhibitor, it effectively disrupts the translation process by targeting the mRNA cap structure. This reagent is valuable for research applications exploring gene expression, translational regulation, and the mechanisms of RNA processing. -
Purine Nucleoside Analog
N-Benzoyl-5′-O-[bis(4-methoxyphenyl)phenylmethyl]-3′-deoxyadenosine is a purine nucleoside analog that exhibits significant antitumor properties. This compound primarily targets malignant lymphoid tissues, exerting its effects through mechanisms such as inhibition of DNA synthesis and induction of apoptosis. It serves as a valuable tool for research applications focused on cancer therapeutics and the exploration of nucleoside analogs in oncological studies. -
Purine Nucleoside Analog
2’-O-(2-Methoxyethyl)-2-aminoadenosine functions as a purine nucleoside analog. It exhibits significant antitumor activity, particularly against indolent lymphoid malignancies. The underlying anticancer mechanisms involve the inhibition of DNA synthesis and the induction of apoptosis, making it a valuable tool for research in cancer biology and therapeutic development. -
Purine Nucleoside Analog
2-(n-Propylidene hydrazino) adenosine is a purine nucleoside analog that exhibits significant antitumor activity, specifically against indolent lymphoid malignancies. Its primary mechanisms of action involve the inhibition of DNA synthesis and the induction of apoptosis, making it a useful tool in cancer research and therapeutic development. This compound supports studies focused on the mechanisms of cancer cell proliferation and survival. -
Purine Nucleoside Analog
2,6-Dichloro-9-(2-c-methyl-2,3,5-tri-O-benzoyl-beta-D-ribofuranosyl)purine is a purine nucleoside analog that exerts its biological activity by interfering with DNA synthesis. This compound is noted for its broad-spectrum antitumor efficacy, particularly against indolent lymphoid malignancies. Its mechanisms of action include the induction of apoptosis and other pathways critical for cancer cell proliferation suppression, making it a valuable tool for cancer research. -
Nucleoside Metabolite
Avenastenone is a nucleoside metabolite with significant implications in cellular metabolism. This compound exhibits potential biological activity by participating in nucleic acid synthesis and influencing metabolic pathways. It is valuable for research applications focused on understanding nucleotide metabolism and cellular proliferation mechanisms. -
Adenosine Analog
8-Bromo-5’-O-(4-cyanobenzyl)-2’,3’-di-O-isopropylidene adenosine is an adenosine analog that primarily targets adenosine receptors. This compound exhibits smooth muscle vasodilatory activity and has potential applications in cancer research due to its ability to inhibit cancer progression. Its structural modifications make it a valuable tool for studying adenosine signaling pathways in various biological systems. -
Purine Nucleoside Analog
N1-Methyl-5-methyl ara-uridine is a purine nucleoside analog known for its broad antitumor activity, particularly against indolent lymphoid malignancies. This compound exerts its anticancer effects primarily through the inhibition of DNA synthesis and the induction of apoptosis. Its application in research includes studying potential therapeutic strategies for lymphoid cancers and examining the underlying mechanisms of nucleoside analog efficacy in tumor cell lines. -
Purine Nucleoside Analog
5-Furan-2-yl-2'-O-methyl uridine functions as a purine nucleoside analog with significant biological activity against indolent lymphoid malignancies. This compound exerts its anticancer effects primarily through the inhibition of DNA synthesis and the induction of apoptosis. Its potential applications in research include the investigation of cancer therapeutics and the study of nucleoside metabolism in various biological systems. -
Adenosine Analog
8-Azidoadenosine is an adenosine analog that primarily functions as a smooth muscle vasodilator and exhibits potential anti-cancer properties. This compound serves as a versatile click chemistry reagent, featuring an azide group that allows it to engage in copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions with alkyne-containing molecules. Additionally, it can participate in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with DBCO or BCN functionalized substrates, making it valuable for applications in bioconjugation and labeling studies in chemical biology research. -
Nucleoside Metabolite
Carbamic acid is a nucleoside metabolite involved in various biological processes. It plays a crucial role in the biosynthesis and metabolism of nucleotides, serving as an important intermediate. This compound is valuable for research applications related to nucleic acid chemistry and cellular signaling pathways. -
Purine Nucleoside Analog
4-Chloro-7-(2-β-C-methyl-β-D-ribofuranosyl)-7H-pyrrolo[2,3-d] pyrimidine is a purine nucleoside analog that exhibits significant antitumor activity, particularly against indolent lymphoid malignancies. Its anticancer effects primarily involve inhibition of DNA synthesis and the induction of apoptosis in cancer cells. This compound is valuable for research focused on the development and evaluation of novel antineoplastic agents. -
Purine Nucleoside Analog
2-Chloro-N6-(2-hydroxyethyl)adenosine is a purine nucleoside analog that demonstrates significant antitumor activity, particularly against indolent lymphoid malignancies. Its primary mechanisms involve the inhibition of DNA synthesis and the induction of apoptosis, making it a valuable tool in cancer research and therapeutics. This compound can be utilized to investigate cellular responses to purine metabolism disruption and to explore novel treatment strategies for lymphoid malignancies. -
Thymidine Analog
5’-O-Acetyl-5-acetyloxymethyluridine is a thymidine analog that exhibits insertional activity in replicated DNA. This compound can be utilized to label cells, enabling the tracking of DNA synthesis and providing valuable insights into cellular proliferation and genomic stability. Its unique properties make it a useful tool in molecular biology and cancer research applications. -
Purine Nucleoside Analog
N6-Benzoyl-2'-chloro-5'-O-(4,4'-dimethoxytrityl)-2'-deoxyadenosine is a purine nucleoside analog that demonstrates significant antitumor activity, particularly against indolent lymphoid malignancies. Its mechanisms of action include inhibition of DNA synthesis and induction of apoptosis, making it valuable for research in cancer therapy. This compound serves as a critical tool for investigating the roles of purine metabolism and nucleoside signaling in oncogenesis. -
Purine Nucleoside Analog
9-(2'-Deoxy-2'-fluoro-β-D-arabinofuranosyl)-9H-purine is a purine nucleoside analog that exerts its biological activity by inhibiting DNA synthesis. This compound demonstrates broad antitumor effects, particularly against indolent lymphoid malignancies, through mechanisms such as the induction of apoptosis. It is a valuable reagent for research applications focused on cancer biology and therapeutic development. -
Purine Nucleoside Analog
6-Chloro-9-(2,3,5-tri-O-benzoyl-2-C-methyl-beta-D-ribofuranosyl)-9H-purine is a purine nucleoside analog known for its potent antitumor properties. This compound targets indolent lymphoid malignancies, exerting its effects primarily through the inhibition of DNA synthesis and the induction of apoptosis. It serves as a valuable tool in cancer research, aiding in the study of therapeutic strategies against various malignancies. -
Hypoxanthine Analog
6-O-Methylinosine is a hypoxanthine analogue that serves as a key metabolite in purine metabolism. It exhibits significant anti-inflammatory properties and has potential as an endogenous inhibitor of poly(ADP-ribose) polymerase (PARP), contributing to cytoprotection by preventing PARP activity. This compound also offers insights into cellular responses to hypoxia, making it valuable for research in cellular signaling and oxidative stress. -
Uridine Analog
3’-β-C-Ethynyluridine is a uridine analog that serves as an important tool in neurological research. It exhibits potential antiepileptic properties and is utilized to investigate anticonvulsant and anxiolytic activities, contributing to the development of novel antihypertensive agents. Additionally, due to its alkyne group, 3’-β-C-Ethynyluridine functions as a click chemistry reagent, allowing for copper-catalyzed azide-alkyne cycloaddition (CuAAc) with azide-containing molecules. -
Purine Nucleoside Analog
4’-Methyl-5-methyluridine is a purine nucleoside analog known for its antitumor properties. This compound exhibits significant activity against indolent lymphoid malignancies, primarily through the inhibition of DNA synthesis and the induction of apoptosis. It serves as a valuable tool in cancer research, contributing to studies focused on therapeutic strategies for lymphoid tumors. -
Adenosine Analog
2'-O-t-Butyldimethylsilyladenosine is an adenosine analog that primarily targets adenosine receptors. This compound functions as a smooth muscle vasodilator and has demonstrated potential in inhibiting cancer progression. It is valuable for research applications in vascular biology and oncology, contributing to studies on therapeutic pathways involving adenosine signaling. -
Purine Nucleoside Analog
8-Bromo-3'-deoxy-3'-fluoroguanosine is a purine nucleoside analog that exhibits significant antitumor activity, particularly against indolent lymphoid malignancies. Its mechanism of action primarily involves the inhibition of DNA synthesis and the induction of apoptosis in cancer cells. This compound is valuable for research related to cancer biology and therapeutic development. -
Purine Nucleoside Analog
2-Aminopurine-9-beta-D-(3’,5’-di-O-benzoyl-2’-deoxy-2’-fluoro)arabinoriboside is a purine nucleoside analog that selectively targets key pathways in cellular proliferation. This compound demonstrates significant antitumor activity, particularly against indolent lymphoid malignancies, by inhibiting DNA synthesis and inducing apoptosis. Its unique structure allows for enhanced interaction with nucleic acids, making it a valuable tool for cancer research and therapeutic development. -
Polymer
9,10-Epoxy-18-hydroxyoctadecanoic acid is a fundamental component of cutin, a polymer that plays a crucial role in plant defense. By forming a protective barrier, this compound minimizes pathogen infiltration and enhances waterproofing of leaves and fruits. It is significant for research in plant biology, particularly in studies focusing on plant resilience and response mechanisms to environmental stressors. -
Adenosine Analog
2-Benzylthioadenosine is an adenosine analog that primarily acts on adenosine receptors. It is known for its vasodilatory effects on smooth muscle and has been investigated for its potential to inhibit cancer progression. This compound is valuable in research applications related to cardiovascular health and oncology, contributing to the understanding of adenosine signaling pathways. -
Purine Nucleoside Analog
2'-O-Acetyl-3',5'-bis-O-benzoyl-6-aza-xylo uridine is a purine nucleoside analog that exhibits significant antitumor activity, particularly against indolent lymphoid malignancies. Its anticancer effects are primarily attributed to the inhibition of DNA synthesis and the induction of apoptosis. This compound serves as a valuable tool for researchers investigating the mechanisms of cancer treatment and the development of therapeutic strategies targeting DNA replication and cellular apoptosis pathways. -
Purine Nucleoside Analog
2',3'-Di-O-acetyl-D-uridine is a purine nucleoside analog that serves as a potential antitumor agent. It exhibits significant biological activity by inhibiting DNA synthesis and inducing apoptosis, making it relevant for research into treatment strategies for indolent lymphoid malignancies. This compound is useful for studying the mechanisms of cancer cell proliferation and therapeutic resistance in various malignancies. -
Thymidine Analog
5-Benzylamino carbonyl-3'-O-acetyl-2'-O-methyl-5'-O-DMTr-uridine is a thymidine analog that exhibits insertional activity in replicated DNA. This compound serves as a valuable tool for labeling cells and monitoring DNA synthesis. Its structural modifications enhance its utility in various molecular biology applications, including studies on nucleic acid dynamics and cellular proliferation. -
Nucleoside Metabolite
2-Hydroxy-3-(4-hydroxyphenyl)propenoate, a nucleoside metabolite, is characterized by its ability to influence various biochemical pathways. This compound exhibits significant biological activity, particularly in metabolic processes associated with nucleoside derivatives. It serves as a valuable tool for research applications focused on metabolic regulation and the study of nucleoside metabolism. -
Purine Nucleoside Analog
3'-N-Acetyl-3'-amino-3'-deoxy-2',5'-di-O-acetyluridine is a purine nucleoside analog known for its broad antitumor activity against indolent lymphoid malignancies. Its primary mechanisms involve the inhibition of DNA synthesis and the induction of apoptosis in cancer cells. This compound holds significant potential for research applications in cancer biology and therapeutic development. -
Nucleoside Metabolite
17-Hydroxylinolenic acid is a nucleoside metabolite involved in cellular signaling pathways. It has been shown to exert anti-inflammatory effects and modulate lipid metabolism. This compound is particularly valuable in research applications focused on understanding metabolic disorders and the role of fatty acids in cellular functions. -
Nucleoside Metabolite
19-Oxotestosterone is a nucleoside metabolite that plays a significant role in androgen metabolism. This compound is useful for studying hormone regulation, particularly in relation to testosterone synthesis and its biological effects. Research applications include investigations into steroidogenesis and the modulation of androgen receptor activity in various biological systems. -
Guanosine Analog
N2-iso-Butyryl-2'-O-(2-methoxyethyl)guanosine is a guanosine analog with immunostimulatory properties. It is capable of inducing type I interferons in certain animal models, thereby exhibiting antiviral effects. The efficacy of this compound is linked to its activation of Toll-like receptor 7 (TLR7), making it a valuable tool for studying immune responses and potential therapeutic applications in viral infections. -
Adenosine Analog
N6-Benzoyl-2',3'-isopropylidene adenosine is an adenosine analog targeting adenosine receptors. This compound exhibits significant smooth muscle vasodilatory activity and has demonstrated potential in inhibiting cancer progression. Its applications in research include studying vascular physiology and cancer biology, making it a valuable tool in the investigation of therapeutic strategies involving adenosine modulation. -
Cytidine Analog
N4-Benzoyl-7’-O-(4,4’-dimethoxytrityloxy)morpholinocytosine is a cytidine analog that functions primarily as an inhibitor of DNA methyltransferases. This compound exhibits potential anti-metabolic and anti-tumor activities, making it valuable for research applications in the study of epigenetic regulation and cancer biology. Its unique structural modifications enhance its stability and bioavailability, facilitating the investigation of cellular processes and therapeutic interventions. -
Purine Nucleoside Analog
Rev 2’-O-MOE-5MeU-5’-amidite is a purine nucleoside analog that target DNA synthesis pathways. This compound exhibits significant anticancer activity, particularly against indolent lymphoid malignancies, by inducing apoptosis and inhibiting cell proliferation. It is a valuable tool for research applications in cancer biology and therapeutic development. -
Purine Nucleoside Analog
2’-O-Acetyl-5’-O-(p-toluoyl)-3’-deoxy-3’-fluoro-5-trifluoromethyluridine is a purine nucleoside analog that exhibits significant antitumor activity, particularly against indolent lymphoid malignancies. Its mechanism of action involves the inhibition of DNA synthesis and the induction of apoptosis, making it a valuable tool for cancer research and therapeutic development. This compound serves as an effective reagent in studies focused on targeting nucleoside metabolism and exploring anticancer strategies. -
Guanosine Analog
5’(R)-C-Methylguanosine is a guanosine analog that serves as a potent immunostimulatory agent. It has been shown to induce type I interferons in various animal models, thereby exhibiting significant antiviral properties. Additionally, the biological activity of this compound is closely linked to the activation of Toll-like receptor 7 (TLR7), making it valuable in research applications focused on immune response and antiviral therapies. -
Purine Nucleoside Analog
2-Amino-9-(2-deoxy-2-fluoro-β-D-arabinofuranosyl)-9H-purine is a purine nucleoside analog that exhibits significant antitumor activity, particularly against indolent lymphoid malignancies. Its primary mechanism of action involves the inhibition of DNA synthesis and the induction of apoptosis in malignant cells. This compound is valuable for research applications focused on cancer biology and therapeutic strategies targeting nucleoside metabolism. -
Phospho Amino Acid
Erythro-5-Phosphooxy-L-lysine is a phospho amino acid that serves as a key intermediate in various biochemical pathways. This compound is primarily involved in cellular signaling and can influence protein interactions and activities through phosphorylation. Its applications in research include studying phospholipid metabolism, protein phosphorylation events, and the role of phospho amino acids in cellular regulation and signaling mechanisms. -
Purine Nucleoside Analog
1,N6-Etheno-9-(β-D-xylofuranosyl)adenosine is a purine nucleoside analog that exhibits significant antitumor activity, particularly against indolent lymphoid malignancies. Its mechanism involves the inhibition of DNA synthesis and the induction of apoptosis, making it a valuable tool in cancer research. This compound can be utilized in studies focused on understanding and targeting tumor cell proliferation and survival pathways. -
Tricarboxylic Acid
(2Z,4E)-5-Hydroxypenta-2,4-diene-1,2,5-tricarboxylic acid is a tricarboxylic acid that demonstrates potential as a biochemical modulator. This compound is of interest for its ability to participate in metabolic pathways, particularly in the regulation of cellular energy states. It has applications in biochemical research, particularly in studies concerning metabolic diseases and the functioning of the tricarboxylic acid cycle. -
Purine Toxin
Py-MAA-Val-Cit-PAB-DX8951 is a purine toxin that functions as an intermediate in the synthesis of antibody-drug conjugates. This compound is instrumental in developing targeted therapies, enhancing the efficacy of anticancer treatments, and improving specificity towards malignant cells. Its utilization in chemical research facilitates advancements in bioconjugation techniques and drug delivery systems. -
Antieoplastic Agent
Flurocitabine, a fluorinated analog of cytosine arabinoside, acts as an antineoplastic agent by undergoing partial hydrolysis in vivo to produce two active metabolites: arabinosyl-fluorocytosine (ara-FC) and arabinosyl-fluorouracil (ara-FU). This compound demonstrates significant antitumor activity and has shown promise in phase I clinical studies for acute leukemia and various solid tumors. Its unique mechanism of action makes Flurocitabine a valuable tool for cancer research and therapy development. -
Guanosine Analog
3’-β-C-Ethynylguanosine is a guanosine analog that acts as an immunostimulatory agent by inducing type I interferons, thereby exhibiting antiviral properties. Its efficacy is linked to the activation of Toll-like receptor 7 (TLR7), which plays a critical role in immune response. Additionally, this compound features an alkyne functional group, making it suitable for click chemistry applications, specifically copper-catalyzed azide-alkyne cycloaddition (CuAAc) with azide-containing molecules, facilitating the study of biochemical interactions. -
Purine Nucleoside Analog
3’,5’-Di-O-benzoyl-2’-deoxy-2’-fluoro-3-Deaza-arabinouridine is a purine nucleoside analog that exhibits significant antitumor activity against indolent lymphoid malignancies. Its mechanism of action involves the inhibition of DNA synthesis and the induction of apoptosis in cancer cells, making it valuable for research into novel anticancer therapies. This compound serves as a crucial tool for investigating cellular responses and therapeutic strategies in oncology. -
Purine Nucleoside Analog
2-Amino-2'-deoxy-N6,N6-dimethyl-2'-adenosine is a purine nucleoside analog that exhibits potent antitumor properties, particularly against indolent lymphoid malignancies. Its mechanism of action involves the inhibition of DNA synthesis and the induction of apoptosis in cancer cells. This compound serves as a valuable tool for research applications focused on understanding cancer biology and therapeutic strategies in oncology. -
Purine Nucleoside Analog
2'-O-Me-2-thio-U-3'-phos phoramidite is a purine nucleoside analog that plays a crucial role in molecular biology research. This compound exhibits significant antitumor activity, particularly against indolent lymphoid malignancies, by inhibiting DNA synthesis and inducing apoptosis. It is valuable for studies focused on cancer treatment and therapeutic development.
